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Structure of 2306245-02-1
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This chiral piperidine derivative features a fluorinated, hydroxylated core with defined stereochemistry at the 3- and 4-positions. The hydrochloride salt enhances solubility and stability for use in synthetic medicinal chemistry. It serves as a key building block for bioactive molecules requiring constrained amine functionality and polar handle integration.
(3R,4R)-3-Fluoropiperidin-4-ol hydrochloride serves as a stereochemically defined building block for fluorinated piperidine scaffolds prevalent in medicinal chemistry. Its bench-stable hydrochloride salt facilitates handling and purification, while the 3-fluoro and 4-hydroxyl groups enable directed functionalization via nucleophilic substitution or oxidation reactions. This configuration supports predictable conformational control in target molecules, making it valuable for synthesizing bioactive compounds requiring defined stereochemistry and metabolic stability.
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Lot numbers can be found on the outside label of a product: